Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
Mercedes-Benz is recalling 2020 GLB 250 vehicles because water may enter the foot wells, potentially causing electrical damage, engine stalls, or a blank instrument cluster.
Nissan recalls 2021 INFINITI QX50 and other vehicles due to front steering knuckles and rear axle housings with insufficient strength from improper heat treatment, which could deform on impact and cause loss of steering control or wheel separation.
BMW is recalling 1999-2001 3 Series vehicles because the driver-side air bag inflator may explode or underinflate, posing a risk of serious injury.
Hi Tech Pharmaceuticals is recalling Isomorph 28 Pure Whey Isolate dietary supplements because FDA inspections found undeclared milk, wheat, and soy.
Simkins Brothers Sweets is recalling Natural Way Almond Butter due to potential undeclared peanuts. Consumers should check for lot #505721.
Biopsybell S.R.L. is recalling 500 units of the Cement Mixing System, Vertebroplasty-Kyphoplasty, Ref VCF-1051, because products labeled as sterile may not have been sterilized.
Biopsybell is recalling 50 units of 11G Direct Single Access devices labeled as sterile but potentially not sterilized, distributed in Mississippi and Kentucky.
Hi Tech Pharmaceuticals is recalling Isomorph 28 Pure Whey Isolate Chocolate Fudge Pop dietary supplements because FDA inspections found undeclared milk, wheat, and soy.
Boston Scientific is recalling VICI RDS Venous Stent Systems manufactured between May 2018 and April 2021 due to reports of stent migration after implantation.
Basic Grain Products Inc is recalling Caramel Rice Cakes sold under Kroger and Stop & Shop brands because the product contains undeclared milk.
Bit & Bet LLC is recalling Thumbs Up 7 Blue 69K capsules because FDA analysis found unapproved sildenafil and tadalafil.
Faribault Foods is recalling O Organics Organic Black Beans because of compromised hermetic seals on the cans. Consumers should check their pantry for the specific UPC and best-by date.
Thor Motor Coach is recalling certain 2022 Sequence, Rize, Scope, and Tellaro recreational vehicles. The Flex-190 solar panel junction box may experience electrical shorts, increasing the fire risk.
Bioseal Corporation is recalling 140 units of Chest Tube Insertion Trays because the included ChloraPrep applicator may allow Aspergillus penicillioides growth, potentially breaching package integrity.
Biopsybell S.R.L. is recalling 75 units of 10 Gauge Drills labeled as sterile that may not have been sterilized.
Biopsybell S.R.L. is recalling CEMIX Cement Mixing Systems labeled as sterile because they may not have been sterilized.
Biopsybell S.R.L. is recalling 5 units of the BPB medica CEMIX cement mixing system because products labeled as sterile may not have been sterilized.
Teva Pharmaceuticals is recalling specific lots of Haloperidol Decanoate Injection because the company cannot guarantee the product is sterile.
Pfizer is recalling 49,525 vials of Sterile Water for Injection because an insect was found in one vial. The product is distributed nationwide.
Hyobin LLC is recalling Triple SupremeZen Plus 3500 capsules because FDA analysis found the unapproved drug tadalafil. The product was marketed without an approved NDA or ANDA.
Biopsybell is recalling 8G Direct Working Cannula Bevel Tips labeled as sterile that may not have been sterilized. The recall affects 30 units distributed in Mississippi and Kentucky.
Biopsybell S.R.L. is recalling 625 units of 10 Gauge Direct Unilateral Stylets because they were labeled as sterile but may not have been sterilized.
Teva Pharmaceuticals is recalling specific lots of Metoclopramide Injection because there is a lack of assurance of sterility. The product was distributed nationwide.
BPB medica is recalling 10 units of RENOVA SPINE kyphoplasty cannulas labeled as sterile but potentially not sterilized. The recall covers distribution in Mississippi and Kentucky.
Daimler Trucks North America is recalling 2019 Freightliner M2 Business Class vehicles with 14Xe ePowertrains because insufficiently crimped stator wires may cause overheating and loss of drive power.